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Plos One|September 17, 2013
Meal frequencies modify the effect of common genetic variants on body mass index in adolescents of the northern Finland birth cohort 1986Anne Jääskeläinen, Ursula Schwab, Marjukka Kolehmainen, et al.
Stem Cell Research|March 30, 2018
Generation of an induced pluripotent stem cell (iPSC) line from a patient with maturity-onset diabetes of the young type 3 (MODY3) carrying a hepatocyte nuclear factor 1-alpha (HNF1A) mutationFrank Griscelli, Hélène Ezanno, Mathis Soubeyrand, et al.
Iscience|August 17, 2021
Signatures of TSPAN8 variants associated with human metabolic regulation and diseasesTisham De, Angela Goncalves, Doug Speed, et al.
Diabetes, Obesity & Metabolism|April 11, 2023
Control of human pancreatic beta cell kinome by glucagon-like peptide-1 receptor biased agonismJiannan Xiao, Liliane El Eid, Teresa Buenaventura, et al.
Diabetologia|June 5, 2014
Type 2 diabetes-related genetic risk scores associated with variations in fasting plasma glucose and development of impaired glucose homeostasis in the prospective DESIR studyMartine Vaxillaire, Loïc Yengo, Stéphane Lobbens, et al.
Adipocyte|May 24, 2013
Evidence for tuning adipocytes ICER levels for obesity careSaška Brajkovic, Raphael Marenzoni, Dimitri Favre, et al.
Clinical Epigenetics|May 16, 2020
Histone deacetylase 9 promoter hypomethylation associated with adipocyte dysfunction is a statin-related metabolic effectAmna Khamis, Raphael Boutry, Mickaël Canouil, et al.
Diabetes|September 28, 2004
Kir6.2 mutations are a common cause of permanent neonatal diabetes in a large cohort of French patientsMartine Vaxillaire, Céline Populaire, Kanetee Busiah, et al.
Diabetes|November 28, 2002
A quantitative trait locus influencing type 2 diabetes susceptibility maps to a region on 5q in an extended French familyLisa J Martin, Anthony G Comuzzie, Sophie Dupont, et al.
Human Molecular Genetics|March 2, 2011
TCF7L2 splice variants have distinct effects on beta-cell turnover and functionOlivier Le Bacquer, Luan Shu, Marion Marchand, et al.
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